Stagi Stefano, Ricci Franco, Bianconi Martina, Sammarco Maria Amina, Municchi Giovanna, Toni Sonia, Lenzi Lorenzo, Verrotti Alberto, de Martino Maurizio
Department of Health Sciences, University of Florence, Anna Meyer Children's University Hospital, Florence 50139, Italy.
Department of Paediatrics, University of Siena, Siena 53100, Italy; gmunicchi@technet.
Nutrients. 2017 May 20;9(5):524. doi: 10.3390/nu9050524.
Pharmacological treatment of obesity and glucose-insulin metabolism disorders in children may be more difficult than in adults. Thus, we evaluate the effects of metformin in comparison with metformin plus a polysaccharide complex (Policaptil Gel Retard, PGR) on body weight and metabolic parameters in obese children and adolescents with metabolic syndrome (MetS). : We retrospectively collected 129 children and adolescents (67 girls, 62 boys; median age 12.6 years) treated for a minimum of two years with metformin and low glycemic index (LGI) diet. Of these, 71 patients were treated with metformin plus PGR after at least 12 months of metformin alone. To minimize the confounding effect of the LGI on auxological and metabolic parameters, the patients were compared with age-, sex-, and BMI-matched control group with obesity and MetS (51 subjects; 24 males, 27 females) treated only with a LGI diet. Assessments included lipids, glucose and insulin (fasting and after oral glucose tolerance test) concentrations. The Homeostatic Model Assessment of Insulin Resistance (HOMA-IR), Matsuda, insulinogenic and disposition indices were calculated. Metformin treatment led to a significant reduction in BMI SDS ( < 0.0001), with a significant difference in ΔBMI SDS between patients and controls ( < 0.0001). Moreover, metformin treated patients showed a reduction in HOMA-IR ( < 0.0001), HbA1c levels ( < 0.0001) and a significant increase in Matsuda index ( < 0.0001) in respect to the reduction discovered in controls ( < 0.05). Moreover, in contrast to the group treated with metformin alone and controls, patients treated with metformin plus PGR showed a further reduction in BMI SDS ( < 0.0001), HOMA-IR ( < 0.0001), HbA1c ( < 0.0001), total, HDL and LDL cholesterol ( < 0.0001), as well as an increase in Matsuda ( < 0.0001), disposition ( < 0.005) and insulinogenic (respectively, < 0.05 and < 0.0001) indices. Metformin appears to show short-term efficacy in reducing BMI, adiposity and glucose and insulin parameters in obese children and adolescents with MetS. However, PGR added to metformin may be useful to potentiate weight loss and to improve glucose-insulin metabolism and adiposity parameters in these patients.
儿童肥胖及糖-胰岛素代谢紊乱的药物治疗可能比成人更困难。因此,我们比较了二甲双胍与二甲双胍加一种多糖复合物(Policaptil Gel Retard,PGR)对患有代谢综合征(MetS)的肥胖儿童和青少年体重及代谢参数的影响。我们回顾性收集了129名儿童和青少年(67名女孩,62名男孩;中位年龄12.6岁),他们接受二甲双胍和低血糖指数(LGI)饮食治疗至少两年。其中,71名患者在单独使用二甲双胍至少12个月后接受了二甲双胍加PGR治疗。为尽量减少LGI对生长发育和代谢参数的混杂影响,将这些患者与年龄、性别和BMI匹配的肥胖及MetS对照组(51名受试者;24名男性,27名女性)进行比较,后者仅接受LGI饮食治疗。评估包括血脂、血糖和胰岛素(空腹及口服葡萄糖耐量试验后)浓度。计算胰岛素抵抗稳态模型评估(HOMA-IR)、松田指数、胰岛素生成指数和处置指数。二甲双胍治疗导致BMI SDS显著降低(<0.0001),患者与对照组之间的ΔBMI SDS存在显著差异(<0.0001)。此外,与对照组相比,接受二甲双胍治疗的患者HOMA-IR降低(<0.0001)、糖化血红蛋白水平降低(<0.0001),松田指数显著升高(<0.0001)(对照组降低<0.05)。此外,与单独使用二甲双胍治疗组和对照组相比,接受二甲双胍加PGR治疗的患者BMI SDS进一步降低(<0.0001)、HOMA-IR降低(<0.0001)、糖化血红蛋白降低(<0.0001)、总胆固醇、高密度脂蛋白胆固醇和低密度脂蛋白胆固醇降低(<0.0001),同时松田指数升高(<0.0001)、处置指数升高(<0.005)以及胰岛素生成指数升高(分别为<0.05和<0.0001)。二甲双胍似乎在降低患有MetS的肥胖儿童和青少年的BMI、肥胖程度以及血糖和胰岛素参数方面显示出短期疗效。然而,在二甲双胍基础上加用PGR可能有助于增强这些患者的体重减轻效果,并改善糖-胰岛素代谢及肥胖参数。